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Clinically determined type of (18)F-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer

PURPOSE: To investigate the association between clinical PET (positron emission tomography) type and oncologic outcome in resectable pancreatic cancer. METHODS: Between January 2008 and October 2012, patients who underwent potentially curative resection for resectable pancreatic ductal adenocarcinom...

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Detalles Bibliográficos
Autores principales: Chong, Jae Uk, Hwang, Ho Kyoung, Lee, Jin Ho, Yun, Mijin, Kang, Chang Moo, Lee, Woo Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325284/
https://www.ncbi.nlm.nih.gov/pubmed/28235029
http://dx.doi.org/10.1371/journal.pone.0172606
Descripción
Sumario:PURPOSE: To investigate the association between clinical PET (positron emission tomography) type and oncologic outcome in resectable pancreatic cancer. METHODS: Between January 2008 and October 2012, patients who underwent potentially curative resection for resectable pancreatic ductal adenocarcinoma without neoadjuvant treatment were retrospectively investigated. Clinical PET type was defined as follows: pancreatic cancer with similar (18)FDG uptake to renal calyx was determined as kidney-type (K-type), and relatively lower (18)FDG uptake than that of renal calyx was regarded as Non-K type. RESULTS: A total of 53 patients were enrolled. After agreement-based reclassification, agreement based K-type (aK-type) was noted in 34 patients (64.2%), and agreement based Non-K type (aNon K-type) was found in 19 patients (35.8%). There was a significant difference between aK-type and aNon K-type pancreatic cancer (tumor size (P = 0.030), adjusted CA 19–9 (P = 0.007), maximum standard uptake value (SUV(max),P<0.001), metabolic tumor volume (MTV(2.5), P<0.001), total lesion glycolysis (TLG, P<0.001)). K-type pancreatic cancer (n = 31) showed a significantly shorter disease-free time compared with Non-K type (n = 16) (10.8 vs. 24.1 months, P = 0.013). It was also noted that aK-type showed inferior disease-free survival to that of aNon-K type pancreatic cancer (11.9 vs. 28.6 months, P = 0.012). CONCLUSIONS: Clinical PET type is a reliable clinical marker to estimate aggressive tumor biology and can be utilized in predicting tumor recurrence and necessity for postoperative chemotherapy.